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Primary hepatic neuroendocrine carcinoma: report of two cases and literature review
BACKGROUND: Primary hepatic neuroendocrine carcinoma (PHNEC) is extremely rare. The diagnosis of PHNEC remains challenging—partly due to its rarity, and partly due to its lack of unique clinical features. Available treatment options for PHNEC include surgical resection of the liver tumor(s), radioth...
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| Vydáno v: | BMC Clin Pathol |
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| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5831736/ https://ncbi.nlm.nih.gov/pubmed/29507528 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12907-018-0070-7 |
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